IP Library Granted Patent US 6,844,192
Granted Patent B2
US 6,844,192 · App. 09/895,940 · Granted Jan 18, 2005

Adenovirus E4 protein variants for virus production

Assignee: Wake Forest University
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Quick Facts
Patent No.
US 6,844,192
App. No.
09/895,940
Granted
Jan 18, 2005
Kind
B2
Abstract

A method of packaging a recombinant viral vector is carried out by: (a) providing a packaging cell, the packaging cell containing and expressing a nucleic acid encoding a mutant adenovirus E4orf6 protein, the E4orf6 protein containing at least one mutation that renders the protein non-toxic to the host cell; (b) transfecting or infecting the packaging cell with a nucleic acid that encodes a recombinant viral vector (e.g., an adenovirus vector or an adeno-associated virus vector), where the vector lacks a functional gene encoding E4orf6 protein; (c) culturing the transfected cells; and then (d) collecting packaged recombinant viral vector from the cultured cells. Nucleic acids, vectors and packaging cells used for carrying out the methods, as well as proteins utilized in the methods, are also described.

Claims (28)

1. A method of packaging a recombinant viral vector, comprising the steps of:

(a) providing a packaging cell, said packaging cell containing and expressing a nucleic acid encoding a mutant adenovirus E4orf6 protein, said E4orf6 protein containing at least one mutation in the region encoding amino acids 230 to 260 wherein said at least one mutation comprises a substitution mutation at position 240, 241, 243, 244, 248, or 251;

(b) transfecting or infecting said packaging cell with a nucleic acid that encodes a recombinant viral vector selected from the group consisting of adenovirus vectors and adeno- associated virus vectors, wherein said vector lacks a functional gene encoding E4orf6 protein; and wherein said mutation renders said mutant adenovirus E4orf6 protein non-toxic to said transfected cells;

(c) culturing said transfected cells under conditions that permit expression of the mutant E4orf6 protein and the production of packaged recombinant viral vector therein: and then

(d) collecting packaged recombinant viral vector from said cultured cells.

2. The method according to claim 1 , wherein said mutation disrupts the interaction of the E4orf6 protein and the E1B-55kDa protein in said host cell.

3. The method according to claim 1 , wherein said packaging cell is transiently transfected with said nucleic acid encoding said mutant adenovirus E4orf6 protein.

4. The method according to claim 1 , wherein said packaging cell is stably transfected with said nucleic acid encoding said mutant adenovirus E4orf6 protein.

5. The method according to claim 1 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 gene is carried by a plasmid, bacteriophage, cosmid or retrovirus.

6. The method according to claim 1 , in which said at least one substitution mutation is a substitution of arginine for an amino acid selected from the group consisting of glutamic acid, aspartic acid, serine, threonine, alanine and glutamine.

7. The method according to claim 1 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 protein encodes (i) an arginine 241 to glutamic acid substitution mutation, (ii) an arginine 243 to glutamic acid substitution mutation, or (iii) both an arginine 241 to glutamic acid substitution mutation and an arginine 243 to glutamic acid substitution mutation.

8. The method according to claim 1 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 protein encodes (i) an arginine 240 to glutamic acid substitution mutation, (ii) an arginine 251 to glutamic acid substitution mutation, or (iii) both an arginine 240 to glutamic acid substitution mutation and an arginine 251 to glutaniic acid substitution mutation.

9. The method according to claim 1 , wherein said viral vector is an adenovirus vector.

10. The method according to claim 1 , wherein said viral vector is an adeno-associated virus vector.

11. A packaging cell, said packaging cell containing and expressing a nucleic acid encoding a mutant adenovirus E4orf6 protein, said E4orf protein containing at least one mutation in the region encoding amino acids 230 to 260 wherein said at least one mutation comprises a substitution mutation at position 240, 241, 243, 244, 248, or 251 that renders said protein non-toxic to a host cell in which said protein is expressed.

12. The packaging cell according to claim 11 , wherein said at least one mutation disrupts the interaction of the E4orf6 protein with the E1B-55kDa protein in a host cell.

13. The packaging cell according to claim 11 , wherein said packaging cell is stably transfected with said nucleic acid encoding said mutant adenovirus E4orf6 protein.

14. The packaging cell according to claim 11 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 protein is carried by a plasmid, bacteriophage, cosmid or retrovirus.

15. The packaging cell according to claim 11 , in which said at least one substitution mutation is a substitution of arginine for an amino acid selected from the group consisting of glutamic acid, aspartic acid, serine, threonine, alanine and glutamine.

16. The packaging cell according to claim 11 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 gene encodes (i) an arginine 241 to glutamic acid substitution mutation, (ii) an arginine 243 to glutamic acid substitution mutation, or (iii) both an arginine 241 to glutamic acid substitution mutation and an arginine 243 to glutamic acid substitution mutation.

17. The packaging cell according to claim 11 , wherein said nucleic acid encoding said mutant adenovirus E4orf6 gene encodes (i) an arginine 240 to glutamic acid substitution mutation, (ii) an arginine 251 to glutamic acid substitution mutation, or (iii) both an arginine 240 to glutamic acid substitution mutation and an arginine 251 to glutamic acid substitution mutation.

18. A nucleic acid encoding a mutant adenovirus E4orf6 protein, said E4orf6 protein containing at least one mutation in the region encoding amino acids 230 to 260 wherein said at least one mutation comprises a substitution mutation at position 240, 241, 243, 244, 248, or 251 that renders said protein non-toxic to a host cell in which said protein is expressed.

19. The nucleic acid according to claim 18 , in which said at least one mutation disrupts the interaction of the E4orf6 protein with the E1B-55kDa protein in a host cell.

20. The nucleic acid according to claim 18 , wherein said nucleic acid is a DNA.

21. The nucleic acid according to claim 18 , wherein said nucleic acid is a plasmid, bacteriophage, plasmid or retrovirus.

22. The nucleic acid according to claim 18 , in which said sat least one substitution mutation is a substitution of arginine for an amino acid selected from the group consisting of glutaniic acid, aspartic acid, serine, threonine, alanine and glutamine.

23. The nucleic acid according to claim 18 , wherein said nucleic acid encodes (i) an arginine 241 to glutamic acid substitution mutation, (ii) an arginine 243 to glutamic acid substitution mutation, or (iii) both an arginine 241 to glutamic acid substitution mutation and an arginine 243 to glutamic acid substitution mutation.

24. The nucleic acid according to claim 18 , wherein said nucleic encodes (i) an arginine 240 to glutamic acid substitution mutation, (ii) an arginine 251 to glutamic acid substitution mutation, or (iii) both an arginine 240 to glutamic acid substitution mutation and an arginine 251 to glutamic acid substitution mutation.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2003
From: WAKE FOREST UNIVERSITY
To: WAKE FOREST UNIVERSITY HEALTH SCIENCES
Reel/Frame 014484/0839 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2001
From: ORLANDO, JOSEPH S.; ORNELLES, DAVID A.
To: WAKE FOREST UNIVERSITY
Reel/Frame 012240/0341 →
Continuity (1)
Related Publication 20030082811A1 · May 1, 2003